Andrew McQuillin

69.9k citations

106 papers · 2.7k indexed · h-index 31

Genetics top 1%
Molecular Biology top 10%
Psychiatry and Mental health top 2%
Cellular and Molecular Neuroscience top 5%
Cognitive Neuroscience top 5%

Co-authors: Hugh Gurling David Curtis Nicholas Bass Sally I. Sharp Jacob Lawrence Gursharan Kalsi Mie Rizig Radhika Kandaswamy
Topics: Genetic Associations and Epidemiology (33 papers)Genetics and Neurodevelopmental Disorders (28 papers)Bipolar Disorder and Treatment (25 papers)
Cited by: Biological Psychiatry Psychiatry and Mental health Genetics
Journals: Nature Communications PLoS ONE American Journal of Psychiatry
Partner nations: United Kingdom United States Germany

In The Last Decade

Andrew McQuillin

101 papers receiving 2.7k citations

Peers

Countries citing papers authored by Andrew McQuillin

Since Specialization

Citations

This map shows the geographic impact of Andrew McQuillin's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Andrew McQuillin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrew McQuillin more than expected).

Fields of papers citing papers by Andrew McQuillin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew McQuillin. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Andrew McQuillin. The network helps show where Andrew McQuillin may publish in the future.

Co-authorship network of co-authors of Andrew McQuillin

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew McQuillin. A scholar is included among the top collaborators of Andrew McQuillin based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Andrew McQuillin. Andrew McQuillin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Genome-wide association studies and cross-population meta-analyses investigating short and long sleep duration 2023 ·Nature Communications ·(unknown),Daniel F. Levey,Olga Giannakopoulou,Joseph D. Deak,Marco Galimberti,(unknown),Hang Zhou,Spiros Denaxas,(unknown),Karoline Kuchenbaecker,Andrew McQuillin,(unknown),John Concato,Daniel J. Buysse,J. Michael Gaziano,Daniel J. Gottlieb,Renato Polimanti,Murray B. Stein,Elvira Bramon,Joel Gelernter	17
2	A machine learning case–control classifier for schizophrenia based on DNA methylation in blood 2021 ·Translational Psychiatry ·Chathura Gunasekara,Eilís Hannon,Harry A. Mackay,Cristian Coarfa,Andrew McQuillin,David St Clair,Jonathan Mill,Robert A. Waterland	14
3	Identifying risk factors involved in the common versus specific liabilities to substance use: A genetically informed approach 2020 ·Addiction Biology ·Eleonora Iob,Tabea Schoeler,Charlotte A. M. Cecil,Esther Walton,Andrew McQuillin,Jean‐Baptiste Pingault	8
4	Predictive power of the ADHD GWAS 2019 polygenic risk scores in independent samples of bipolar patients with childhood ADHD 2019 ·Journal of Affective Disorders ·Maria Grigoroiu‐Serbânescu,Giovanni Giaroli,Johan H. Thygesen,(unknown),Tim B. Bigdeli,Nicholas Bass,Carmen C. Diaconu,Ana Iulia Neagu,Andreas J. Forstner,Franziska Degenhardt,Stefan Herms,Markus M. Nöthen,Andrew McQuillin	13
5	Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia 2017 ·Annals of Human Genetics ·(unknown),Alessia Fiorentino,Sally I. Sharp,Niamh L. O’Brien,(unknown),Giovanni Giaroli,David Curtis,Nicholas Bass,Andrew McQuillin	16
6	Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia 2017 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Ganna Leonenko,Alexander Richards,James Walters,Andrew Pocklington,Kimberly Chambert,(unknown),Sally I. Sharp,Niamh L. O’Brien,David Curtis,Nicholas Bass,Andrew McQuillin,Christina M. Hultman,Jennifer L. Moran,Steven A. McCarroll,Pamela Sklar,Benjamin M. Neale,Peter Holmans,Michael J. Owen,Patrick F. Sullivan,Michael O’Donovan	16
7	OC-031 A Genome-Wide Association Study Identifies PNPLA3 and SLC38A4 as Risk Loci for Alcoholic Hepatitis 2016 ·Stephen J. Atkinson,(unknown),Andrew McQuillin,(unknown),Mark Thursz,(unknown)	1
8	Allelic association, DNA resequencing and copy number variation at the metabotropic glutamate receptor GRM7 gene locus in bipolar disorder 2014 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Radhika Kandaswamy,Andrew McQuillin,David Curtis,Hugh Gurling	32
9	Does rare matter? Copy number variants at 16p11.2 and the risk of psychosis: A systematic review of literature and meta-analysis 2014 ·Schizophrenia Research ·Giovanni Giaroli,Nicholas Bass,André Strydom,(unknown),Andrew McQuillin	33
10	Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder 2011 ·Psychiatric Genetics ·Gregory Lydall,Nicholas Bass,Andrew McQuillin,Jacob Lawrence,Adebayo Anjorin,Radhika Kandaswamy,A C Pereira,Irene Guerrini,David Curtis,(unknown),Pamela Sklar,Shaun Purcell,Hugh Gurling	51
11	Case–case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes 2010 ·Psychiatric Genetics ·David Curtis,(unknown),Andrew McQuillin,Nicholas Bass,A C Pereira,Radhika Kandaswamy,Jacob Lawrence,Adebayo Anjorin,Khalid Choudhury,Susmita Datta,Vinay Puri,Robert Krasucki,Jonathan Pimm,Srinivasa Thirumalai,Digby Quested,Hugh Gurling	58
12	Genetics of attention-deficit hyperactivity disorder (ADHD) 2009 ·Neuropharmacology ·Sally I. Sharp,Andrew McQuillin,Hugh Gurling	99
13	A Genomewide Association Study of Response to Lithium for Prevention of Recurrence in Bipolar Disorder 2009 ·American Journal of Psychiatry ·Roy H. Perlis,Jordan W. Smoller,Manuel A. R. Ferreira,Andrew McQuillin,Nicholas Bass,Jacob Lawrence,Roy H. Perlis,Vishwajit L. Nimgaonkar,Edward M. Scolnick,Hugh Gurling,Pamela Sklar,Shaun Purcell	105
14	A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia 2008 ·Molecular Psychiatry ·Susmita Datta,Andrew McQuillin,Mie Rizig,Ekaterini Blaveri,Srinivasa Thirumalai,Gursharan Kalsi,Jacob Lawrence,Nicholas Bass,Vinita Puri,Khalid Choudhury,J Pimm,Caroline Crombie,G. T. Fraser,Nicholas Walker,David Curtis,Marketa Zvelebil,A C Pereira,Radhika Kandaswamy,David St Clair,Hugh Gurling	45
15	Identification of the Slynar Gene (AY070435) and Related Brain Expressed Sequences as a Candidate Gene for Susceptibility to Affective Disorders Through Allelic and Haplotypic Association With Bipolar Disorder on Chromosome 12q24 2006 ·American Journal of Psychiatry ·Gursharan Kalsi,Andrew McQuillin,Birte Degn,(unknown),Nicholas Bass,Jacob Lawrence,Khalid Choudhury,Vinay Puri,Mette Nyegaard,David Curtis,Ole Mors,Torben A. Kruse,(unknown),Hugh Gurling	11
16	Genetic linkage analysis supports the presence of two susceptibility loci for alcoholism and heavy drinking on chromosome 1p22.1-11.2 and 1q21.3-24.2. 2005 ·BMC Genetics ·Irene Guerrini,Christopher C. H. Cook,(unknown),(unknown),Andrew McQuillin,David Curtis,(unknown)	32
17	A novel polymorphism in exon 11 of the WKL1 gene, shows no association with schizophrenia 2002 ·European Journal of Human Genetics ·Andrew McQuillin,Gursharan Kalsi,(unknown),(unknown),Soraya Mayet,Digby Quested,Philip N. Baker,David Curtis,Hugh Gurling	13
18	Genome wide linkage anlaysis supports the presence of two separate susceptibility loci on chromosome 1q32 for biopolar disorder and 1q21-22.3 for schizophrenia 2000 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Hugh Gurling,David Curtis,G. Kalsi,Andrew McQuillin,Jacob Lawrence,P. Murphy,Jon Brynjolfsson,M. G. McInnis,(unknown),Hannes Pétursson	1
19	Adjacent genetic markers on chromosome 11p15.5 at or near the tyrosine hydroxylase locus that show population linkage disequilibrium with each other do not show allelic association with bipolar affective disorder 1999 ·Psychological Medicine ·Andrew McQuillin,Jacob Lawrence,David Curtis,G. Kalsi,(unknown),(unknown),H. Gurling	8
20	Localization of Functional Regions of the Cucumber Mosaic Virus RNA Replicase Using Monoclonal and Polyclonal Antibodies 1994 ·Journal of General Virology ·R. J. Hayes,Vini Pereira,Andrew McQuillin,K. W. Buck	17

About Andrew McQuillin

Andrew McQuillin is a scholar working on Genetics, Psychiatry and Mental health and Pathology and Forensic Medicine, having authored 106 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (33 papers), Genetics and Neurodevelopmental Disorders (28 papers) and Bipolar Disorder and Treatment (25 papers). The work is most often cited by research in Biological Psychiatry (199 citations), Psychiatry and Mental health (772 citations) and Genetics (1.2k citations). Andrew McQuillin has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Hugh Gurling, David Curtis, Nicholas Bass, Sally I. Sharp, Jacob Lawrence, Gursharan Kalsi, Mie Rizig, Radhika Kandaswamy, Hannes Pétursson and Khalid Choudhury. Their work appears in journals such as Nature Communications, PLoS ONE and American Journal of Psychiatry.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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